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Dexmedetomidine an Effective Drug in Reducing Anesthetic Requirements in External Dacrocystorhinostomy (DCR) Patients

R

Research Institute of Ophthalmology, Egypt

Status and phase

Enrolling
Phase 1

Conditions

Patients Undergoing External Dacrocystorhinostomy Operations
Assess Decreased Anesthetic Requirements Intraoperative

Treatments

Drug: Dexmedetomidine Hydrochloride

Study type

Interventional

Funder types

Other

Identifiers

NCT06808295
24-11-17-6-5

Details and patient eligibility

About

Assessing the intra and postoperative hemodynamic stability in patients undergoing external dacrocystorhinostomy under general anesthesia using Dexmedetomidine as a preoperative sedation compared to traditional technique with intraoperative analgesia and assessing decreased anesthetic requirements intra and postoperative

Full description

Dexmedetomidine is a highly selective alpha 2 adrenoceptor agonist, having characteristics of natural sleep like sedation, can reduce pain intensity and opioid consumption without influencing the time of recovery from general anesthesia

Enrollment

24 estimated patients

Sex

All

Ages

16 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

patients of both sexes 16 years to 75 years of age ASA (American society of Anesthesiologists) I-III

Exclusion criteria

  • Pediatric age group
  • ASA more than III

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

Dexmedetomidine
Active Comparator group
Description:
Dexmedetomidine 0.25 microgram per kilogram is used in Dacrocystorhinostomy patients 20 minutes before induction of general anesthesia
Treatment:
Drug: Dexmedetomidine Hydrochloride
Control
No Intervention group
Description:
Fentanyl as an analgesic is used with general anesthesia in Dacrocystorhinostomy patients

Trial contacts and locations

1

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Central trial contact

Dina Moustafa Mohamed Ali, MD

Data sourced from clinicaltrials.gov

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